Irinotecan plus fluorouracil/leucovorin for metastatic colorectal cancer: A new survival standard Journal Article


Authors: Saltz, L. B.; Douillard, J. Y.; Pirotta, N.; Alakl, M.; Gruia, G.; Awad, L.; Elfring, G. L.; Locker, P. K.; Miller, L. L.
Article Title: Irinotecan plus fluorouracil/leucovorin for metastatic colorectal cancer: A new survival standard
Abstract: Background. Irinotecan is a topoisomerase I inhibitor that prolongs survival in patients with colorectal cancer refractory to fluorouracil (5-FU) and leucovorin (LV). This demonstrated activity of irinotecan as effective second-line therapy for colorectal cancer led to evaluation of combination irinotecan/5-FU/LV as first-line therapy for patients with metastatic disease. The results of two prospective phase III randomized, controlled, multicenter, multinational clinical trials in patients with previously untreated metastatic colorectal cancer served as the basis for U.S. and European approval of irinotecan/5-FU/LV for this indication. An overview of the findings of these two pivotal studies provides insights regarding the application of this new combination in clinical practice. Methods. Patients were randomly assigned to receive 5-FU/LV, either alone, or with concurrent irinotecan. The study conducted primarily in North America (study 1), employed bolus 5-FU/LV schedules, while the study performed primarily in Europe (study 2), employed infusional 5-FU/LV regimens. Major endpoints included tumor response rate, time to tumor progression (TTP), overall survival, quality of life, and safety. Results. In study 1, the respective confirmed response rates for irinotecan/5-FU/LV versus 5-FU/LV were 39% and 21% (p < .001); median TTPs were 7.0 months and 4.3 months, respectively (p = .004). In study 2, response rates for irinotecan/5-FU/LV versus 5-FU/LV alone were 35% and 22% (p = .005); median TTPs were 6.7 months and 4.4 months, respectively (p < .001). Survival time increased significantly with irinotecan/5-FU/LV versus 5-FU/LV alone in both studies (study 1: median 14.8 months versus 12.6 months, p = .042; study 2: median 17.4 months versus 14.1 months, p = .032). The combined analysis of the data from the two studies showed median survivals of 15.9 months versus 13.3 months, favoring the irinotecan-containing combinations (stratified-by-study p = .003). Patients in study 1 had a 36% lower risk of tumor progression and a 20% lower risk of death with the irinotecan combination than with 5-FU/LV alone; comparable risk reduction values in study 2 were 42% and 23%. While grade 3 diarrhea and vomiting were more common with irinotecan/5-FU/LV, grade 4 neutropenia, neutropenic fever, and mucositis were less common with irinotecan/5-FU/LV than with the Mayo Clinic 5-FU/LV regimen. Conclusion. The combination of irinotecan/5-FU/LV is superior to 5-FU/LV alone as first-line therapy for patients with metastatic colorectal cancer, offering consistently improved tumor control and prolonged survival. Irinotecan-based combination therapy sets a new survival standard for the treatment of this life-threatening disease.
Keywords: adult; cancer survival; controlled study; treatment outcome; aged; aged, 80 and over; middle aged; survival analysis; major clinical study; clinical trial; neutropenia; review; fluorouracil; cancer combination chemotherapy; diarrhea; drug safety; antineoplastic agents; drug approval; clinical practice; colorectal cancer; metastasis; quality of life; controlled clinical trial; mucosa inflammation; randomized controlled trial; vomiting; antineoplastic combined chemotherapy protocols; antineoplastic agents, phytogenic; camptothecin; irinotecan; febrile neutropenia; colorectal neoplasms; randomized controlled trials; multicenter study; folinic acid; neoplasm metastasis; phase 3 clinical trial; tumor growth; dna topoisomerase inhibitor; leucovorin; humans; prognosis; human; male; female; priority journal
Journal Title: The Oncologist
Volume: 6
Issue: 1
ISSN: 1083-7159
Publisher: Oxford University Press  
Date Published: 2001-02-01
Start Page: 81
End Page: 91
Language: English
DOI: 10.1634/theoncologist.6-1-81
PUBMED: 11161231
PROVIDER: scopus
DOI/URL:
Notes: Export Date: 21 May 2015 -- Source: Scopus
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  1. Leonard B Saltz
    790 Saltz